Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: RDH5[original query] |
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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Nature genetics 2013 Mar 45 (3): 314-8. Verhoeven Virginie J M, Hysi Pirro G, Wojciechowski Robert, Fan Qiao, Guggenheim Jeremy A, Höhn René, MacGregor Stuart, Hewitt Alex W, Nag Abhishek, Cheng Ching-Yu, Yonova-Doing Ekaterina, Zhou Xin, Ikram M Kamran, Buitendijk Gabriëlle H S, McMahon George, Kemp John P, Pourcain Beate St, Simpson Claire L, Mäkelä Kari-Matti, Lehtimäki Terho, Kähönen Mika, Paterson Andrew D, Hosseini S Mohsen, Wong Hoi Suen, Xu Liang, Jonas Jost B, Pärssinen Olavi, Wedenoja Juho, Yip Shea Ping, Ho Daniel W H, Pang Chi Pui, Chen Li Jia, Burdon Kathryn P, Craig Jamie E, Klein Barbara E K, Klein Ronald, Haller Toomas, Metspalu Andres, Khor Chiea-Chuen, Tai E-Shyong, Aung Tin, Vithana Eranga, Tay Wan-Ting, Barathi Veluchamy A, , Chen Peng, Li Ruoying, Liao Jiemin, Zheng Yingfeng, Ong Rick T, Döring Angela, , Evans David M, Timpson Nicholas J, Verkerk Annemieke J M H, Meitinger Thomas, Raitakari Olli, Hawthorne Felicia, Spector Tim D, Karssen Lennart C, Pirastu Mario, Murgia Federico, Ang Wei, , Mishra Aniket, Montgomery Grant W, Pennell Craig E, Cumberland Phillippa M, Cotlarciuc Ioana, Mitchell Paul, Wang Jie Jin, Schache Maria, Janmahasatian Sarayut, Janmahasathian Sarayut, Igo Robert P, Lass Jonathan H, Chew Emily, Iyengar Sudha K, , Gorgels Theo G M F, Rudan Igor, Hayward Caroline, Wright Alan F, Polasek Ozren, Vatavuk Zoran, Wilson James F, Fleck Brian, Zeller Tanja, Mirshahi Alireza, Müller Christian, Uitterlinden André G, Rivadeneira Fernando, Vingerling Johannes R, Hofman Albert, Oostra Ben A, Amin Najaf, Bergen Arthur A B, Teo Yik-Ying, Rahi Jugnoo S, Vitart Veronique, Williams Cathy, Baird Paul N, Wong Tien-Yin, Oexle Konrad, Pfeiffer Norbert, Mackey David A, Young Terri L, van Duijn Cornelia M, Saw Seang-Mei, Bailey-Wilson Joan E, Stambolian Dwight, Klaver Caroline C, Hammond Christopher |
Association between ZIC2, RASGRF1, and SHISA6 genes and high myopia in Japanese subjects. Investigative ophthalmology & visual science 2013 Nov 54 (12): 7492-7. Oishi Maho, Yamashiro Kenji, Miyake Masahiro, Akagi-Kurashige Yumiko, Kumagai Kyoko, Nakata Isao, Nakanishi Hideo, Yoshikawa Munemitsu, Oishi Akio, Gotoh Norimoto, Tsujikawa Akitaka, , Yamada Ryo, Matsuda Fumihiko, Yoshimura Nagahi |
Comprehensive replication of the relationship between myopia-related genes and refractive errors in a large Japanese cohort. Investigative ophthalmology & visual science 2014 Nov 55 (11): 7343-54. Yoshikawa Munemitsu, Yamashiro Kenji, Miyake Masahiro, Oishi Maho, Akagi-Kurashige Yumiko, Kumagai Kyoko, Nakata Isao, Nakanishi Hideo, Oishi Akio, Gotoh Norimoto, Yamada Ryo, Matsuda Fumihiko, Yoshimura Nagahisa, |
Evaluation of 12 myopia-associated genes in Chinese patients with high myopia. Investigative ophthalmology & visual science 2015 Feb 56 (2): 722-9. Li Jiali, Jiang Dan, Xiao Xueshan, Li Shiqiang, Jia Xiaoyun, Sun Wenmin, Guo Xiangming, Zhang Qingjio |
Next-generation sequencing-based comprehensive molecular analysis of 43 Japanese patients with cone and cone-rod dystrophies. Molecular vision 2016 22 150-60. Oishi Maho, Oishi Akio, Gotoh Norimoto, Ogino Ken, Higasa Koichiro, Iida Kei, Makiyama Yukiko, Morooka Satoshi, Matsuda Fumihiko, Yoshimura Nagahi |
Genome-wide association analyses identify 139 loci associated with macular thickness in the UK Biobank cohort.
Human molecular genetics 2019 04 28 (7): 1162-1172. Gao X Raymond, Huang Hua, Kim Heej |
Potential Mutations in Chinese Pathologic Myopic Patients and Contributions to Phenotype. Current molecular medicine 2019 2 18 (10): 689-697. Chen L, Wei Y, Chi W, Fang D, Jiang X, Zhang |
Genetic Analysis of Consanguineous Pakistani Families with Congenital Stationary Night Blindness. Ophthalmic research 2021 11 65 (1): 104-110. Azhar Baig Hafiz Muhammad, Ansar Muhammad, Iqbal Afia, Naeem Muhammad Asif, Quinodoz Mathieu, Calzetti Giacomo, Iqbal Muhammad, Rivolta Car |
A Novel Pathogenic Variant in the RDH5 Gene in a Patient with Fundus Albipunctatus and Severe Macular Atrophy. Case reports in genetics 2022 4 2022 1183772. You Hyelin, Sierpina Dav |
Novel variants in the RDH5 Gene in a Chinese Han family with fundus albipunctatus. BMC ophthalmology 2022 2 22 (1): 69. Qian Tianwei, Gong Qiaoyun, Shen Hangqi, Li Caihua, Wang Gao, Xu Xun, Schrauwen Isabelle, Wang Weij |
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- Page last updated:Apr 22, 2024
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